Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86656004 | HCID 86656004 | — |
| Solvent | Dimethyl Carbonate | HCID 12021 | — |
| Product | HCID 86656003 | HCID 86656003 | 98% |
Reaction Steps
41.5 g (0.409 mol) of triethylamine was added to 300 ml of dimethyl carbonate solution of 44.0 g (0.386 mol) of 4-formyloxy-2-butyn-1-ol, and cooled to 0° C. 46.9 g (0.409 mol) of methanesulfonyl chloride was dropwise added to the solution while the inner temperature was controlled to be not higher than 15° C. After the addition, this was stirred at 25° C. for 1.5 hours, the reaction mixture was poured into an aqueous saturated sodium bicarbonate solution, the aqueous layer was separated, and the organic layer was concentrated to give 72.6 g (yield 98%) 4-formyloxy-2-butyn-1-yl methanesulfonate. For use in the battery test, this was purified through silica gel column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383274B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-cace5d0197254a189049ee2bdbac4450 |
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| Source note | uspto-grants-2013_02 |
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